GB978547A - New thiophene derivatives, process for their preparation and their use - Google Patents
New thiophene derivatives, process for their preparation and their useInfo
- Publication number
- GB978547A GB978547A GB29793/63A GB2979363A GB978547A GB 978547 A GB978547 A GB 978547A GB 29793/63 A GB29793/63 A GB 29793/63A GB 2979363 A GB2979363 A GB 2979363A GB 978547 A GB978547 A GB 978547A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxazole ring
- carbon atoms
- compound
- acid
- acids
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 150000003577 thiophenes Chemical class 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 8
- 125000002971 oxazolyl group Chemical group 0.000 abstract 8
- 125000004432 carbon atom Chemical group C* 0.000 abstract 6
- 150000001555 benzenes Chemical class 0.000 abstract 4
- -1 polyhexamethylene Polymers 0.000 abstract 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 abstract 3
- 229920002678 cellulose Polymers 0.000 abstract 3
- 150000002191 fatty alcohols Chemical class 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- 239000001913 cellulose Substances 0.000 abstract 2
- 239000007859 condensation product Substances 0.000 abstract 2
- 239000003599 detergent Substances 0.000 abstract 2
- 150000002170 ethers Chemical class 0.000 abstract 2
- 230000003287 optical effect Effects 0.000 abstract 2
- 229920000151 polyglycol Polymers 0.000 abstract 2
- 239000010695 polyglycol Substances 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 abstract 2
- 239000000344 soap Substances 0.000 abstract 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 abstract 2
- WNKQDGLSQUASME-UHFFFAOYSA-N 4-sulfophthalic acid Chemical compound OC(=O)C1=CC=C(S(O)(=O)=O)C=C1C(O)=O WNKQDGLSQUASME-UHFFFAOYSA-N 0.000 abstract 1
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- 239000004952 Polyamide Substances 0.000 abstract 1
- 239000002202 Polyethylene glycol Substances 0.000 abstract 1
- 239000004793 Polystyrene Substances 0.000 abstract 1
- 239000004372 Polyvinyl alcohol Substances 0.000 abstract 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 230000002378 acidificating effect Effects 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 229920000180 alkyd Polymers 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 239000012736 aqueous medium Substances 0.000 abstract 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical class N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 abstract 1
- 150000001556 benzimidazoles Chemical group 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 abstract 1
- 239000004327 boric acid Substances 0.000 abstract 1
- 238000005282 brightening Methods 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 229920006218 cellulose propionate Polymers 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 abstract 1
- 239000002270 dispersing agent Substances 0.000 abstract 1
- 239000004744 fabric Substances 0.000 abstract 1
- 239000000194 fatty acid Substances 0.000 abstract 1
- 229930195729 fatty acid Natural products 0.000 abstract 1
- 150000004665 fatty acids Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 239000011261 inert gas Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 abstract 1
- 230000007935 neutral effect Effects 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 235000005985 organic acids Nutrition 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 abstract 1
- 229920001223 polyethylene glycol Polymers 0.000 abstract 1
- 229920000098 polyolefin Polymers 0.000 abstract 1
- 229920000137 polyphosphoric acid Polymers 0.000 abstract 1
- 229920002223 polystyrene Polymers 0.000 abstract 1
- 229920002451 polyvinyl alcohol Polymers 0.000 abstract 1
- 229920000915 polyvinyl chloride Polymers 0.000 abstract 1
- 239000004800 polyvinyl chloride Substances 0.000 abstract 1
- 229920001290 polyvinyl ester Polymers 0.000 abstract 1
- 239000005033 polyvinylidene chloride Substances 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- 229940005657 pyrophosphoric acid Drugs 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical class NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 abstract 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 abstract 1
- 229920002994 synthetic fiber Polymers 0.000 abstract 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 abstract 1
- RAOIDOHSFRTOEL-UHFFFAOYSA-N tetrahydrothiophene Chemical group C1CCSC1 RAOIDOHSFRTOEL-UHFFFAOYSA-N 0.000 abstract 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 abstract 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 abstract 1
- 230000000007 visual effect Effects 0.000 abstract 1
- 239000002699 waste material Substances 0.000 abstract 1
- 235000005074 zinc chloride Nutrition 0.000 abstract 1
- 239000011592 zinc chloride Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/45—Heterocyclic compounds having sulfur in the ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Artificial Filaments (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1014962A CH450342A (de) | 1962-08-27 | 1962-08-27 | Verwendung von neuen Thiophenderivaten als optische Aufhellmittel ausserhalb der Textilindustrie |
Publications (1)
Publication Number | Publication Date |
---|---|
GB978547A true GB978547A (en) | 1964-12-23 |
Family
ID=4359899
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB29793/63A Expired GB978547A (en) | 1962-08-27 | 1963-07-26 | New thiophene derivatives, process for their preparation and their use |
Country Status (9)
Country | Link |
---|---|
US (1) | US3178445A (enrdf_load_stackoverflow) |
AT (1) | AT241406B (enrdf_load_stackoverflow) |
BE (1) | BE636576A (enrdf_load_stackoverflow) |
CH (1) | CH450342A (enrdf_load_stackoverflow) |
DE (1) | DE1253222B (enrdf_load_stackoverflow) |
ES (1) | ES291148A1 (enrdf_load_stackoverflow) |
GB (1) | GB978547A (enrdf_load_stackoverflow) |
NL (2) | NL129024C (enrdf_load_stackoverflow) |
SE (1) | SE302285B (enrdf_load_stackoverflow) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH504471A (de) * | 1963-11-25 | 1971-03-15 | Ciba Geigy Ag | Neues Verfahren zur Herstellung von 7-Aminocephalosporanverbindungen |
CH426721A (de) * | 1964-06-19 | 1967-06-30 | Ciba Geigy | Verwendung von Oxazolverbindungen als optische Aufhellmittel für textile Materialien aus Polyestern |
US3499762A (en) * | 1966-11-03 | 1970-03-10 | Eastman Kodak Co | Photographic elements comprising novel u.v.-absorbing optical brightening agents |
US3449257A (en) * | 1966-11-03 | 1969-06-10 | Eastman Kodak Co | Brightener compositions |
GB1515766A (en) * | 1976-01-30 | 1978-06-28 | British Petroleum Co | Polymeric films having selective light transmissive properties |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL242891A (enrdf_load_stackoverflow) * | 1958-09-02 |
-
0
- BE BE636576D patent/BE636576A/xx unknown
- NL NL297105D patent/NL297105A/xx unknown
- NL NL129024D patent/NL129024C/xx active
-
1962
- 1962-08-27 CH CH1014962A patent/CH450342A/de unknown
-
1963
- 1963-07-25 US US297664A patent/US3178445A/en not_active Expired - Lifetime
- 1963-07-26 GB GB29793/63A patent/GB978547A/en not_active Expired
- 1963-08-26 ES ES291148A patent/ES291148A1/es not_active Expired
- 1963-08-26 DE DEC30781A patent/DE1253222B/de active Pending
- 1963-08-26 AT AT683063A patent/AT241406B/de active
- 1963-08-26 SE SE9298/63A patent/SE302285B/xx unknown
Also Published As
Publication number | Publication date |
---|---|
SE302285B (enrdf_load_stackoverflow) | 1968-07-15 |
NL297105A (enrdf_load_stackoverflow) | |
NL129024C (enrdf_load_stackoverflow) | |
BE636576A (enrdf_load_stackoverflow) | |
CH450342A (de) | 1968-01-31 |
DE1253222B (de) | 1967-11-02 |
ES291148A1 (es) | 1964-02-16 |
AT241406B (de) | 1965-07-26 |
US3178445A (en) | 1965-04-13 |
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